KUMMAS Bipolar Forceps - Indonesia BPOM Medical Device Registration
KUMMAS Bipolar Forceps is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603916705. The device is manufactured by KUMMAS CORPORATION from Pakistan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SOMETECH NEW Zealand.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
KUMMAS CORPORATIONCountry of Origin
Pakistan
Authorized Representative
SOMETECH NEW ZealandAR Address
AKR Tower Lantai 11 Unit 11G dan 11C, Jalan Panjang Nomor 5 ,RT 011 RW 010, Kec. Kebon Jeruk, Kel. Kebon Jeruk, Jakarta Barat, 11530
Registration Date
Jun 21, 2024
Expiry Date
Apr 16, 2029
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
Non Electromedic Non Sterile
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